Protein S exacerbates alcoholic hepatitis by stimulating liver natural killer T cells. (11th December 2014)
- Record Type:
- Journal Article
- Title:
- Protein S exacerbates alcoholic hepatitis by stimulating liver natural killer T cells. (11th December 2014)
- Main Title:
- Protein S exacerbates alcoholic hepatitis by stimulating liver natural killer T cells
- Authors:
- Chelakkot‐Govindalayathil, A.‐L.
Mifuji‐Moroka, R.
D'Alessandro‐Gabazza, C. N.
Toda, M.
Matsuda, Y.
Gil‐Bernabe, P.
Roeen, Z.
Yasuma, T.
Yano, Y.
Gabazza, E. C.
Iwasa, M.
Takei, Y. - Abstract:
- <abstract abstract-type="main" id="jth12789-abs-0001"> <title>Summary</title> <sec id="jth12789-sec-0001" sec-type="section"> <title>Background</title> <p>Alcohol consumption is a major cause of liver injury but the mechanisms are not completely understood. Protein S (PS) is an anticoagulant glycoprotein with multiple functions. The role of PS in liver injury is unknown.</p> </sec> <sec id="jth12789-sec-0002" sec-type="section"> <title>Objectives</title> <p>This study investigated the role of PS in acute alcoholic hepatitis.</p> </sec> <sec id="jth12789-sec-0003" sec-type="section"> <title>Methods</title> <p>A mouse overexpressing human PS (hPS‐TG) was generated in which acute hepatitis was induced by intraperitoneal injection of ethanol.</p> </sec> <sec id="jth12789-sec-0004" sec-type="section"> <title>Results</title> <p>The levels of serum liver enzymes and liver tissue inflammatory cytokines and the degree of hepatic steatosis were significantly increased in hPS‐TG mice treated with ethanol compared with ethanol‐treated wild type (WT) mice. Cell expansion, activation and inhibition of apoptosis were significantly augmented in natural killer T (NKT) cells from hPS‐TG mice compared with WT mice. Liver mononuclear cells from hPS‐TG mice express higher levels of inflammatory cytokines than those from WT mice after stimulation with a specific stimulant of NKT cells <italic>in vitro</italic>. In a co‐culture system of hepatocytes and NKT cells, the effects of PS on<abstract abstract-type="main" id="jth12789-abs-0001"> <title>Summary</title> <sec id="jth12789-sec-0001" sec-type="section"> <title>Background</title> <p>Alcohol consumption is a major cause of liver injury but the mechanisms are not completely understood. Protein S (PS) is an anticoagulant glycoprotein with multiple functions. The role of PS in liver injury is unknown.</p> </sec> <sec id="jth12789-sec-0002" sec-type="section"> <title>Objectives</title> <p>This study investigated the role of PS in acute alcoholic hepatitis.</p> </sec> <sec id="jth12789-sec-0003" sec-type="section"> <title>Methods</title> <p>A mouse overexpressing human PS (hPS‐TG) was generated in which acute hepatitis was induced by intraperitoneal injection of ethanol.</p> </sec> <sec id="jth12789-sec-0004" sec-type="section"> <title>Results</title> <p>The levels of serum liver enzymes and liver tissue inflammatory cytokines and the degree of hepatic steatosis were significantly increased in hPS‐TG mice treated with ethanol compared with ethanol‐treated wild type (WT) mice. Cell expansion, activation and inhibition of apoptosis were significantly augmented in natural killer T (NKT) cells from hPS‐TG mice compared with WT mice. Liver mononuclear cells from hPS‐TG mice express higher levels of inflammatory cytokines than those from WT mice after stimulation with a specific stimulant of NKT cells <italic>in vitro</italic>. In a co‐culture system of hepatocytes and NKT cells, the effects of PS on ethanol‐mediated cell injury were suppressed by a CD1d neutralizing antibody. Alcoholic liver injury was significantly improved in mice pre‐treated with PS siRNA and anti‐protein S antibody compared with control mice. Patients with alcoholic hepatitis showed significantly increased plasma PS levels and enhanced liver expression of PS and CD1d compared with controls.</p> </sec> <sec id="jth12789-sec-0005" sec-type="section"> <title>Conclusions</title> <p>The results of this study suggest that PS exacerbates acute alcoholic hepatitis by inhibiting apoptosis of activated NKT cells.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of thrombosis and haemostasis. Volume 13:Number 1(2015:Jan.)
- Journal:
- Journal of thrombosis and haemostasis
- Issue:
- Volume 13:Number 1(2015:Jan.)
- Issue Display:
- Volume 13, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 13
- Issue:
- 1
- Issue Sort Value:
- 2015-0013-0001-0000
- Page Start:
- 142
- Page End:
- 154
- Publication Date:
- 2014-12-11
- Subjects:
- Thrombosis -- Periodicals
Hemostasis -- Periodicals
Blood coagulation disorders -- Periodicals
616.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1538-7836 ↗
http://www.blackwellpublishing.com/journals/jth ↗
https://www.sciencedirect.com/journal/journal-of-thrombosis-and-haemostasis ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jth.12789 ↗
- Languages:
- English
- ISSNs:
- 1538-7933
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5069.345000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3120.xml